Precision Health Through
Genomic Intelligence
“Advanced genetic analysis technology that links laboratory data to personalized healthcare for individuals and organizations seeking in-depth DNA insights for accurate health analysis and care.”
9K+ happy & healthy clients
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Why AThenaAI?
Automated Analysis Pipeline
An automated system for classifying and identifying genetic information. Transform raw NGS data into clinically meaningful information quickly and accurately using our expert knowledge and a fully automated system. This minimizes human error, saves team time in screening and categorizing genetic data, allowing for greater focus on in-depth analysis. We utilize a globally updated genetic database, ensuring data accuracy, and provide access to over 1,000 Thai case studies, offering the most precise health insights specific to the ASEAN population.
Flexible Support Solution
Our customizable service models cater to your needs and budget, whether for small or large projects. Choose from software-as-a-service (SaaS), full-service (full analysis), or a hybrid approach. We offer convenience, ease of use, and a great experience and you do not even need a team to handle it.
There are Specialists in the Team
We offer more than just software, we have a team of bioinformaticians and genetic experts to provide support and consultation, helping to solve complex technical problems and offering guidance in interpreting difficult-to-interpret data.
Clinical-grade Reporting with AI
We automatically generate clear, easy-to-understand, and clinical-grade analytical reports. AI filters and prioritizes the most relevant clinical data, enabling physicians to make immediate decisions. Our AI assistant further processes and interprets the data, making us a genomic analysis platform that makes health data convenient and easy to use in real-world situations.
Why AThenaAI?
Automated Annotation Pipeline
An automated system for classifying and identifying genetic information. Transform raw NGS data into clinically meaningful information quickly and accurately using our expert knowledge and a fully automated system. This minimizes human error, saves team time in screening and categorizing genetic data, allowing for greater focus on in-depth analysis. We utilize a globally updated genetic database, ensuring data accuracy, and provide access to over 1,000 Thai case studies, offering the most precise health insights specific to the ASEAN population.
Flexible Support Solution
Our customizable service models cater to your needs and budget, whether for small or large projects. Choose from software-as-a-service (SaaS), full-service (full analysis), or a hybrid approach. We offer convenience, ease of use, and a great experience and you don’t even need a team to handle it.
Three are Specialist in the Team
We offer more than just software, we have a team of bioinformaticians and genetics experts to provide support and consultation, helping to solve complex technical problems and offering guidance in interpreting difficult to interpret data.
Clinical-grade Reporting with AI
We automatically generate clear, easy-to-understand, and clinical-grade analytical reports. AI filters and prioritizes the most relevant clinical data, enabling physicians to make immediate decisions. Our AI assistant further processes and interprets the data, making us a genomic analysis platform that makes health data convenient and easy to use in real-world situations.
AI-Powered Bioinformatics Analysis
The first of its kind in Thailand
Advancing Precision Health Through NGS
Next Generation Sequencing
NGS (Next Generation Sequencing) is a revolutionary technology in genetics that enables massive parallel sequencing of DNA and RNA. This technology allows for the simultaneous reading and analysis of vast amounts of genetic information, resulting in significantly faster, more efficient, and lower-cost sequencing compared to traditional methods. NGS is therefore a fundamental technology that supports advanced clinical applications and research.
Whole Exome Sequencing
The method we currently use.
WES (Whole Exome Sequencing) is a targeted genetic analysis strategy that selects and decodes only specific regions of the genome that code for proteins, called “exomes.” Although these make up only about 1-2% of the total genome, they contain crucial information and are directly related to the occurrence of most genetic diseases. It is a highly cost-effective and efficient method for clinical diagnosis because it focuses the analysis on the most likely disease-causing locations, reducing data complexity and interpretation time compared to WGS (Whole Genome Sequencing).
FAQs
HOW LONG DOES IT TAKE TO ANALYZE THE DATA?
Depending on the service and testing method used by the client, it generally takes 4-8 weeks.
HOW WILL I RECEIVE THE TEST RESULTS?
You can view the results report through your account on the AThenaAI application.
WHAT WILL THE REPORT INDICATE, AND HOW CAN I UNDERSTAND IT IF I HAVE NO MEDICAL KNOWLEDGE?
Our report is designed to be easy to understand, includes a summary of health risks, self-care guidelines, and also offers additional online consultations with doctors.
DURING TRANSPORT, WILL THE SALIVA SAMPLE BE DAMAGED BEFORE REACHING THE LAB?
Because we include a custom-developed reagent in the kit, it helps preserve the saliva sample, keeping the DNA intact and undamaged for longer. Temperature control is not required, so damage will not occur. However, we recommend returning the sample within 24 hours.
WHY IS ONLY SALIVA USED FOR DNA TESTING?
Using saliva samples provides sufficient DNA for analysis, with white blood cells being a key DNA source. This method is also simpler, more convenient, and less painful compared to collecting samples from hair or blood.
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